Predictive value of prostate specific antigen in a European HIV-positive cohort: does one size fit all?

Publikation: Bidrag til tidsskriftLetterForskningfagfællebedømt

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Predictive value of prostate specific antigen in a European HIV-positive cohort : does one size fit all? / Shepherd, Leah; Borges, Álvaro H; Ravn, Lene; Harvey, Richard; Bower, Mark; Grulich, Andrew; Silverberg, Michael; Kronborg, Gitte; Galli, Massimo; Kirk, Ole; Lundgren, Jens; Mocroft, Amanda; EuroSIDA in EuroCoord.

I: Antiviral Therapy, Bind 21, Nr. 6, 2016, s. 529-534.

Publikation: Bidrag til tidsskriftLetterForskningfagfællebedømt

Harvard

Shepherd, L, Borges, ÁH, Ravn, L, Harvey, R, Bower, M, Grulich, A, Silverberg, M, Kronborg, G, Galli, M, Kirk, O, Lundgren, J, Mocroft, A & EuroSIDA in EuroCoord 2016, 'Predictive value of prostate specific antigen in a European HIV-positive cohort: does one size fit all?', Antiviral Therapy, bind 21, nr. 6, s. 529-534. https://doi.org/10.3851/IMP3026

APA

Shepherd, L., Borges, Á. H., Ravn, L., Harvey, R., Bower, M., Grulich, A., Silverberg, M., Kronborg, G., Galli, M., Kirk, O., Lundgren, J., Mocroft, A., & EuroSIDA in EuroCoord (2016). Predictive value of prostate specific antigen in a European HIV-positive cohort: does one size fit all? Antiviral Therapy, 21(6), 529-534. https://doi.org/10.3851/IMP3026

Vancouver

Shepherd L, Borges ÁH, Ravn L, Harvey R, Bower M, Grulich A o.a. Predictive value of prostate specific antigen in a European HIV-positive cohort: does one size fit all? Antiviral Therapy. 2016;21(6):529-534. https://doi.org/10.3851/IMP3026

Author

Shepherd, Leah ; Borges, Álvaro H ; Ravn, Lene ; Harvey, Richard ; Bower, Mark ; Grulich, Andrew ; Silverberg, Michael ; Kronborg, Gitte ; Galli, Massimo ; Kirk, Ole ; Lundgren, Jens ; Mocroft, Amanda ; EuroSIDA in EuroCoord. / Predictive value of prostate specific antigen in a European HIV-positive cohort : does one size fit all?. I: Antiviral Therapy. 2016 ; Bind 21, Nr. 6. s. 529-534.

Bibtex

@article{89e2583e30a442fe8ddc079224ab7f3d,
title = "Predictive value of prostate specific antigen in a European HIV-positive cohort: does one size fit all?",
abstract = "BACKGROUND: It is common practice to use prostate specific antigen (PSA) ≥4.0 ng/ml as a clinical indicator for men at risk of prostate cancer (PCa), however, this is unverified in HIV+ men. We aimed to describe kinetics and predictive value of PSA for PCa in HIV+ men.METHODS: A nested case control study of 21 men with PCa and 40 matched-controls within EuroSIDA was conducted. Prospectively stored plasma samples before PCa (or matched date in controls) were measured for the following markers: total PSA (tPSA), free PSA (fPSA), testosterone and sex hormone binding globulin (SHBG). Conditional logistic regression models investigated associations between markers and PCa. Mixed models were used to describe kinetics. Sensitivity and specificity of using tPSA >4 ng/ml to predict PCa was calculated. Receiver operating characteristic curves were used to identify optimal cutoffs in HIV+ men for total PSA.RESULTS: 61 HIV+ men were included with a median 6 (IQR 2-9) years follow-up. Levels of tPSA increased by 13.7% per year (95% CI 10.3, 17.3) in cases, but was stable in controls (-0.4%; 95% CI -2.5, 1.7). Elevated PSA was associated with higher odds of PCa at first (OR for twofold higher 4.7; 95% CI 1.7, 12.9; P<0.01) and last sample (8.1; 95% CI 1.1, 58.9; P=0.04). A similar relationship was seen between fPSA and PCa. Testosterone and SHBG level were not associated with PCa. tPSA level >4 ng/ml had 99% specificity and 38% sensitivity. The optimal PSA cutoff was 1.5 ng/ml overall (specificity =84%, sensitivity =81%).CONCLUSIONS: PSA was highly predictive of PCa in HIV+ men; however, the commonly used PSA>4 ng/ml to indicate high PCa risk was not sensitive in our population and use of the lower cutoff of PSA>1.5 ng/ml warrants consideration.",
author = "Leah Shepherd and Borges, {{\'A}lvaro H} and Lene Ravn and Richard Harvey and Mark Bower and Andrew Grulich and Michael Silverberg and Gitte Kronborg and Massimo Galli and Ole Kirk and Jens Lundgren and Amanda Mocroft and {EuroSIDA in EuroCoord}",
year = "2016",
doi = "10.3851/IMP3026",
language = "English",
volume = "21",
pages = "529--534",
journal = "Antiviral Therapy",
issn = "1359-6535",
publisher = "International Medical Press",
number = "6",

}

RIS

TY - JOUR

T1 - Predictive value of prostate specific antigen in a European HIV-positive cohort

T2 - does one size fit all?

AU - Shepherd, Leah

AU - Borges, Álvaro H

AU - Ravn, Lene

AU - Harvey, Richard

AU - Bower, Mark

AU - Grulich, Andrew

AU - Silverberg, Michael

AU - Kronborg, Gitte

AU - Galli, Massimo

AU - Kirk, Ole

AU - Lundgren, Jens

AU - Mocroft, Amanda

AU - EuroSIDA in EuroCoord

PY - 2016

Y1 - 2016

N2 - BACKGROUND: It is common practice to use prostate specific antigen (PSA) ≥4.0 ng/ml as a clinical indicator for men at risk of prostate cancer (PCa), however, this is unverified in HIV+ men. We aimed to describe kinetics and predictive value of PSA for PCa in HIV+ men.METHODS: A nested case control study of 21 men with PCa and 40 matched-controls within EuroSIDA was conducted. Prospectively stored plasma samples before PCa (or matched date in controls) were measured for the following markers: total PSA (tPSA), free PSA (fPSA), testosterone and sex hormone binding globulin (SHBG). Conditional logistic regression models investigated associations between markers and PCa. Mixed models were used to describe kinetics. Sensitivity and specificity of using tPSA >4 ng/ml to predict PCa was calculated. Receiver operating characteristic curves were used to identify optimal cutoffs in HIV+ men for total PSA.RESULTS: 61 HIV+ men were included with a median 6 (IQR 2-9) years follow-up. Levels of tPSA increased by 13.7% per year (95% CI 10.3, 17.3) in cases, but was stable in controls (-0.4%; 95% CI -2.5, 1.7). Elevated PSA was associated with higher odds of PCa at first (OR for twofold higher 4.7; 95% CI 1.7, 12.9; P<0.01) and last sample (8.1; 95% CI 1.1, 58.9; P=0.04). A similar relationship was seen between fPSA and PCa. Testosterone and SHBG level were not associated with PCa. tPSA level >4 ng/ml had 99% specificity and 38% sensitivity. The optimal PSA cutoff was 1.5 ng/ml overall (specificity =84%, sensitivity =81%).CONCLUSIONS: PSA was highly predictive of PCa in HIV+ men; however, the commonly used PSA>4 ng/ml to indicate high PCa risk was not sensitive in our population and use of the lower cutoff of PSA>1.5 ng/ml warrants consideration.

AB - BACKGROUND: It is common practice to use prostate specific antigen (PSA) ≥4.0 ng/ml as a clinical indicator for men at risk of prostate cancer (PCa), however, this is unverified in HIV+ men. We aimed to describe kinetics and predictive value of PSA for PCa in HIV+ men.METHODS: A nested case control study of 21 men with PCa and 40 matched-controls within EuroSIDA was conducted. Prospectively stored plasma samples before PCa (or matched date in controls) were measured for the following markers: total PSA (tPSA), free PSA (fPSA), testosterone and sex hormone binding globulin (SHBG). Conditional logistic regression models investigated associations between markers and PCa. Mixed models were used to describe kinetics. Sensitivity and specificity of using tPSA >4 ng/ml to predict PCa was calculated. Receiver operating characteristic curves were used to identify optimal cutoffs in HIV+ men for total PSA.RESULTS: 61 HIV+ men were included with a median 6 (IQR 2-9) years follow-up. Levels of tPSA increased by 13.7% per year (95% CI 10.3, 17.3) in cases, but was stable in controls (-0.4%; 95% CI -2.5, 1.7). Elevated PSA was associated with higher odds of PCa at first (OR for twofold higher 4.7; 95% CI 1.7, 12.9; P<0.01) and last sample (8.1; 95% CI 1.1, 58.9; P=0.04). A similar relationship was seen between fPSA and PCa. Testosterone and SHBG level were not associated with PCa. tPSA level >4 ng/ml had 99% specificity and 38% sensitivity. The optimal PSA cutoff was 1.5 ng/ml overall (specificity =84%, sensitivity =81%).CONCLUSIONS: PSA was highly predictive of PCa in HIV+ men; however, the commonly used PSA>4 ng/ml to indicate high PCa risk was not sensitive in our population and use of the lower cutoff of PSA>1.5 ng/ml warrants consideration.

U2 - 10.3851/IMP3026

DO - 10.3851/IMP3026

M3 - Letter

C2 - 26823399

VL - 21

SP - 529

EP - 534

JO - Antiviral Therapy

JF - Antiviral Therapy

SN - 1359-6535

IS - 6

ER -

ID: 164792529